Cruciata Margherita, Sannino Ciro, Ercolini Danilo, Scatassa Maria L, De Filippis Francesca, Mancuso Isabella, La Storia Antonietta, Moschetti Giancarlo, Settanni Luca
Department of Agricultural and Forest Science, Università degli Studi di Palermo, Palermo, Italy.
Appl Environ Microbiol. 2014 Apr;80(7):2050-61. doi: 10.1128/AEM.03837-13. Epub 2014 Jan 17.
The microbial composition of artisan and industrial animal rennet pastes was studied by using both culture-dependent and -independent approaches. Pyrosequencing targeting the 16S rRNA gene allowed to identify 361 operational taxonomic units (OTUs) to the genus/species level. Among lactic acid bacteria (LAB), Streptococcus thermophilus and some lactobacilli, mainly Lactobacillus crispatus and Lactobacillus reuteri, were the most abundant species, with differences among the samples. Twelve groups of microorganisms were targeted by viable plate counts revealing a dominance of mesophilic cocci. All rennets were able to acidify ultrahigh-temperature-processed (UHT) milk as shown by pH and total titratable acidity (TTA). Presumptive LAB isolated at the highest dilutions of acidified milks were phenotypically characterized, grouped, differentiated at the strain level by randomly amplified polymorphic DNA (RAPD)-PCR analysis, and subjected to 16S rRNA gene sequencing. Only 18 strains were clearly identified at the species level, as Enterococcus casseliflavus, Enterococcus faecium, Enterococcus faecalis, Enterococcus lactis, Lactobacillus delbrueckii, and Streptococcus thermophilus, while the other strains, all belonging to the genus Enterococcus, could not be allotted into any previously described species. The phylogenetic analysis showed that these strains might represent different unknown species. All strains were evaluated for their dairy technological performances. All isolates produced diacetyl, and 10 of them produced a rapid pH drop in milk, but only 3 isolates were also autolytic. This work showed that animal rennet pastes can be sources of LAB, mainly enterococci, that might contribute to the microbial diversity associated with dairy productions.
采用依赖培养和不依赖培养的方法,研究了手工制作和工业生产的动物凝乳酶糊剂的微生物组成。针对16S rRNA基因的焦磷酸测序能够在属/种水平上鉴定出361个可操作分类单元(OTU)。在乳酸菌(LAB)中,嗜热链球菌和一些乳酸杆菌,主要是卷曲乳杆菌和罗伊氏乳杆菌,是最丰富的物种,不同样品之间存在差异。通过活菌平板计数法对12组微生物进行了检测,结果显示嗜温球菌占优势。所有凝乳酶都能使超高温处理(UHT)的牛奶酸化,这通过pH值和总可滴定酸度(TTA)得以体现。对酸化牛奶最高稀释度下分离出的推定LAB进行了表型特征分析、分组,并通过随机扩增多态性DNA(RAPD)-PCR分析在菌株水平上进行区分,然后进行16S rRNA基因测序。在种水平上仅明确鉴定出18株菌株,分别为格氏肠球菌、粪肠球菌、屎肠球菌、乳酸肠球菌、德氏乳杆菌和嗜热链球菌,而其他所有属于肠球菌属的菌株无法归入任何先前描述的物种。系统发育分析表明,这些菌株可能代表不同的未知物种。对所有菌株的乳制品技术性能进行了评估。所有分离株都产生双乙酰,其中10株能使牛奶中的pH值迅速下降,但只有3株分离株具有自溶能力。这项研究表明,动物凝乳酶糊剂可能是LAB的来源,主要是肠球菌,它们可能有助于增加与乳制品生产相关的微生物多样性。